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Cites articles 70

Date

Title

Authors

2018-07

Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence

Daniel R. Weinberger, Russell A. Poldrack, Ingrid Melle, Kjetil Sundet, Danielle Posthuma, Aarno Palotie, Robert Plomin, Astri J. Lundervold, Srdjan Djurovic, Ole A. Andreassen, Olav B Smeland, Ivar Reinvang, Sten Linnarsson, Robert Karlsson, Eliza Congdon, Stella Giakoumaki, Edythe D. London, Kenneth Kendler, Swapnil Awasthi, Marianne Nygaard, Sven Stringer, Delilah Zabaneh, Sara Hägg, Jari Lahti, Katri Räikkönen-Talvitie, Ian Deary, Bradley T Webb, Neil Pendleton, Ida Karlsson, Jeanne E. Savage, Peter B. Barr, Jonathan R I Coleman, Anke R Hammerschlag, Joey W. Trampush, Hannah Young, Ornit Chiba-Falek, Nelson A. Freimer, Michael Gill, Bettina Konte, Dave Liewald, Anna C. Need, Panos Roussos, Henning Tiemeier, Gerome Breen, Jens Hjerling-Leffler, M. Arfan Ikram, Sarah E. Medland, Tinca Polderman, Patrick F Sullivan, Margaret J. Wright, Grant W. Montgomery, Sophie van der Sluis, Danielle M. Dick, Ina Giegling, Dan Rujescu, Tyrone Cannon, Ana Belén Muñoz-Manchado, Katherine E Burdick, Julien Bryois, Katrina L Grasby, Chandra A Reynolds, Robert M Bilder, Elizabeth T Cirulli, Gary J. Donohoe, Emily Drabant Conley, Stephanie Le Hellard, Todd Lencz, Matthew A Scult, Vidar M Steen, Richard E Straub, Nancy Pedersen, Mats Nagel, Eva Krapohl, Gunter Schumann, Aiden Corvin, Johan G. Eriksson, Thomas Espeseth, Matthew C Keller, Gonçalo Abecasis, Stephan Ripke, David C. Glahn, Derek W. Morris, Pamela DeRosse, John M Starr, Andrea Christoforou, William Ollier, Panos Bitsios, Dan E Arking, Dimitrios G Avramopoulos, Fred W Sabb, Nick Martin, Max Lam, Antony Payton, Aristotle Voineskos, Alex Hatzimanolis, Nikolaos Smyrnis, Philip R Jansen, Christiaan de Leeuw, Jakob Kaminski, Narelle Hansell, Erin Burke Quinlan, Nathan Skene, Tonya White, Birgit Debrabant, Scott Vrieze
2018-03-21

Measuring and Estimating the Effect Sizes of Copy Number Variants on General Intelligence in Community-Based Samples.

Jean-Baptiste Poline, Eva Loth, Tomáš Paus, Roberto Toro, IMAGEN Consortium
2018-02-27

lme4qtl: linear mixed models with flexible covariance structure for genetic studies of related individuals

Angel Martinez-Perez
2018-04-24

Association of copy number variation across the genome with neuropsychiatric traits in the general population

Anna L Guyatt, Evangelia Stergiakouli, Joanna Martin, James Walters, Michael C O'Donovan, Anita Thapar, Dheeraj Rai, Stanley Zammit, Tom R. Gaunt, George Kirov
2018-02-27

Temporal lobe thickness and verbal memory in first-degree relatives of individuals with schizophrenia.

Keith H. Nuechterlein, Katherine L Narr
2017-10-02

The Genetics of Endophenotypes of Neurofunction to Understand Schizophrenia (GENUS) consortium: A collaborative cognitive and neuroimaging genetics project.

Paola Dazzan, Vince D. Calhoun, Donna Cosgrove, Simone Ciufolini, Tiago Reis Marques, Esther Walton, Jorge Jovicich, Robin Murray, Matcheri S Keshavan, Larry J. Seidman, Stefan Ehrlich, Ina Giegling, René S. Kahn, Wiepke Cahn, Dan Rujescu, Martha E. Shenton, Zora Kikinis, Marek Kubicki, Raquelle I Mesholam-Gately, Donald C Goff, Jordan W Smoller, Dara S Manoach, Robert McCarley, Tracey L Petryshen, Annette M Hartmann, James Walters, Joshua L Roffman, Derek W. Morris, Gary J. Donohoe, Jill M Goldstein, Paul G Nestor, Gabriëlla A M Blokland, Heidi W Thermenos, Bettina Konte, Aristotle Voineskos, Max Lam, Elvira Bramon, Richard S E Keefe, Timothea Toulopoulou, Anthony David, Jessica A. Turner, Marco M. Picchioni, Scott R Sponheim, Erin W Dickie, Nicolas Crossley, Manuela Russo, Valeria Mondelli, Marta Di Forti, M. Aurora Falcone, Neeltje E M van Haren, Antje Annechien Talea Simone Reinders, Rick P F Wolthusen, Aiden Corvin, Shaun M Purcell, Joey W. Trampush, Randy L. Gollub, Sonja M C de Zwarte, Lisa Osiecki, Aine Sinead
2017-05-22

Reevaluation of SNP heritability in complex human traits

David J. Balding, Na Cai, Doug Speed
2017-05-26

Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits

Eleftheria Zeggini, Loz Southam, Arthur Gilly, Jeremy Schwartzentruber, Maria Karaleftheri, George Dedoussis
2016-11-21

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

Sarah E Bergen, Enrico Domenici, Patrik K E Magnusson, Joseph Buxbaum, Erik G Jönsson, Vahram Haroutunian, Tiina Paunio, Thomas Werge, Bhooma Thiruvahindrapuram, Lieuwe de Haan, Inez Myin-Germeys, Benedicto Crespo-Facorro, Sophie E Legge, Stephen W. Scherer, Paola Giusti-Rodríguez, Tracey L Petryshen, Morten Mattingsdal, Joshua L Roffman, Bradley T Webb, Inge Joa, Tune H Pers, Jennifer L. Moran, Elvira Bramon, Murray J Cairns, Rolf Adolfsson, George Kirov, Donald W. Black, David Curtis, Danielle Posthuma, Sven Cichon, Michael C O'Donovan, Peter M. Visscher, Tõnu Esko, Andres Metspalu, Veikko Salomaa, Andrew Pocklington, Brian Kelly, Igor Nenadic, Srdjan Djurovic, Franziska Degenhardt, Ingrid Melle, Juha Veijola, Valentina Escott-Price, Aarno Palotie, Ingrid Agartz, Ole A. Andreassen, Christina M. Hultman, Larry J. Seidman, Kenneth Kendler, Mark Joseph Daly, Frank Dudbridge, Ina Giegling, Ann Olincy, René S. Kahn, Wiepke Cahn, Dan Rujescu, Raquelle I Mesholam-Gately, Jouko Lönnqvist, Jaana Suvisaari, Christos Pantelis, C. Robert Cloninger, Dominique Campion, Naomi R. Wray, Jordan W Smoller, Patrick F. Sullivan, Juha Karjalainen, Nakao Iwata, Jeffrey Lieberman, Johan G. Eriksson, Pamela Sklar, Stephan Ripke, Luba Kalaydjieva, Benjamin M. Neale, Daniele Merico, Rita M. Cantor, Dermot Walsh, Joel N Hirschhorn, John L Waddington, Douglas Blackwood, David St Clair, Michele T Pato, Nancy G. Buccola, James J. Crowley, Gary J. Donohoe, Per Hoffmann, Matthew C Keller, Robert McCarley, Derek W. Morris, Alkes Price, Douglas M. Ruderfer, Thomas G. Schulze, Stephanie H Witt, Aaron R Wolen, Steven A McCarroll, Markus M Nöthen, James Walters, Olli P H Pietiläinen, Nelson A. Freimer, Roel Ophoff, Annette M Hartmann, Eric Strengman, Nick Craddock, Christian Marshall, Daniel P Howrigan, Aniket Shetty, Peter Holmans, Madhusudan Gujral, William M Brandler, Zhouzhi Wang, Karin V Fuentes Fajarado, Margot Albus, Farooq Amin, Joshua R Atkins, Silviu-Alin Bacanu, Richard A Belliveau, Marcelo Bertalan, Elizabeth Bevilacqua, Tim B. Bigdeli, Richard Bruggeman, Brendan Bulik-Sullivan, Guiqing Cai, Vaughan Carr, Noa Carrera, Stanley V Catts, Kimberley D Chambert, Jurgen Del Favero, Dimitris Dikeos, Elodie Drapeau, Jubao Duan, Peter Eichhammer, Laurent Essioux, Kyle Kai-How Farh, Martilias Farrell, Robert Freedman, Andreas J Forstner, Menachem Fromer, Elliot S Gershon, Stephanie Godard, Jacqueline I Goldstein, Jacob Gratten, Marian L Hamshere, Frans A. Henskens, Stefan Herms, Andrea Hofman, Masashi Ikeda, Bettina Konte, Claudine Laurent-Levinson, Deborah M Levy, Carmel M Loughland, Brion S. Maher, Colm Mcdonald, Carin J Meijer, Patricia T Michie, Vihra Milanova, Younes Mokrab, Deborah A Nertney, Gerald Nestadt, Kristin K Nicodemus, Laura Nisenbaum, Annelie Nordin, Colm O'Dushlaine, Jonathan Pimm, Ann E Pulver, Digby Quested, Abraham Reichenberg, Panos Roussos, Alan R. Sanders, Adam J Savitz, Ulrich Schall, Sibylle G Schwab, Edward M Scolnick, Jeremy Silverman, Chris C A Spencer, Eli A Stahl, Jana Strohmaier, T. Scott Stroup, Jin P Szatkiewicz, Srinivas Thirumalai, Paul A Tooney, Mark Weiser, Dieter B Wildenauer, Brandon K Wormley, Clement C. Zai, Aiden Corvin, Pablo V Gejman, Assen V Jablensky, Douglas F Levinson, Andrew McQuillin, Bryan Mowry, Brien P. Riley, Jonathan Sebat, Shaun M Purcell, David Collier, Phil H Lee, Kieran Murphy, Dheeraj Malhotra, Psychosis Endophenotypes International Consortium, James L. Kennedy
2016-08-18

Cognitive Performance Among Carriers of Pathogenic Copy Number Variants: Analysis of 152,000 UK Biobank Subjects

Rhys H Thomas, George Kirov, Mark Einon, Kimberley Kendall, Elliott Rees, Michael C O'Donovan, Valentina Escott-Price
2016-03-10

The complex behavioral phenotype of 15q13.3 microdeletion syndrome

Danielle Guffey, Jill A Rosenfeld, Michael J Gambello, Charles G Minard, Christian P Schaaf, Pawel Stankiewicz
2016-01-01

Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities

Didier Lacombe, Caroline Rooryck, Bogdan Draganski, John E Spiro, Anne M Maillard, Aia E Jønch, Kyle J Steinman, Jacques S Beckmann, Alexandre Reymond, Andres Metspalu, William A. Faucett, Joris Andrieux, David H. Ledbetter
2016-05-15

Investigating the effects of copy number variants on reading and language performance

Alessia Visconti, Alessandro Gialluisi, Mario Falchi, Clyde Francks, Simon Fisher
2016-12-13

Schizophrenia copy number variants and associative learning

George Kirov, Nicholas E Clifton, Andrew Pocklington, Elliott Rees, James Walters, Michael C O'Donovan, Kerrie L Thomas, Jeremy Hall
2015-10-05

Prioritizing Clinically Relevant Copy Number Variation from Genetic Interactions and Gene Function Data

Michael Brudno
2015-09-09

Cognitive intermediate phenotype and genetic risk for psychosis
2015-05-01

Copy number variations and cognitive phenotypes in unselected populations

Reedik Mägi, Erika Salvi, Nicholas J. Timpson, Alexander Teumer, Andres Metspalu, Zoltán Kutalik, Nathan Pankratz, Anne M Maillard, Tom R. Gaunt, Jacques S Beckmann, Alexandre Reymond, Anna L Guyatt, Evelin Mihailov, Matt McGue, William Iacono, Daniele Cusi, Katrin Männik, Aurélien Mace, Hashem A Shihab, Helene Alavere, Anneli Kolk, Anu Reigo, Liis Leitsalu, Anne-Maud Ferreira, Margit Nõukas, Sébastien Jacquemont
2015-11-10

The Number of Genomic Copies at the 16p11.2 Locus Modulates Language, Verbal Memory, and Inhibition

Cédric Le Caignec, Franck Ramus, Anne M Maillard, Bogdan Draganski, Nouchine Hadjikhani, Jacques S Beckmann, Laurent Mottron, Alexandre Reymond, Andres Metspalu
2015-12-23

Verbal memory impairments in schizophrenia associated with cortical thinning
2014-10-11

Does rare matter? Copy number variants at 16p11.2 and the risk of psychosis: a systematic review of literature and meta-analysis

Andrew McQuillin, Andre Strydom
2014-06-01

Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome

Erik Boot, Stephan Eliez, Maria Niarchou, Linda E Campbell, Martin Debbané, Marianne Bernadette van den Bree, Kieran Murphy, Declan Murphy, Raquel E Gur, Abraham Weizman, Donna M McDonald-McGinn, Therese van Amelsvoort, Maude Schneider, Carrie E Bearden, Stephen R. Hooper, Wendy R Kates
2014-04-29

Copy number variation in schizophrenia in Sweden

George Kirov, Michael C O'Donovan, Guanhua Chen, Jennifer L. Moran, Douglas M. Ruderfer, Sarah E Bergen, Patrik K E Magnusson, James J. Crowley, Elliott Rees, James Walters
2014-07-15

Copy number deletion burden is associated with cognitive, structural, and resting-state network differences in patients with schizophrenia.

Andrew Martin, David C. Reutens
2014-01-01

Low-Frequency Copy-Number Variants and General Cognitive Ability: No Evidence of Association

Saonli Basu, Nathan Pankratz, Matt McGue, William Iacono, Robert Kirkpatrick
2013-08-28

The penetrance of copy number variations for schizophrenia and developmental delay

George Kirov, Michael C O'Donovan, Elliott Rees, James Walters, Valentina Escott-Price, Sophie E Legge, Jennifer L. Moran
2013-12-05

Analysis of copy number variations at 15 schizophrenia-associated loci

Michael C O'Donovan, George Kirov, Elliott Rees, James Walters, Anthony R Isles, Sophie E Legge, Jennifer L. Moran
2013-12-18

CNVs conferring risk of autism or schizophrenia affect cognition in controls

Kári Stefánsson, Hreinn Stefansson, Engilbert Sigurdsson, Andreas Meyer-Lindenberg, Gyda Bjornsdottir, Johan Hilge Thygesen, G. Bragi Walters, Shitij Kapur, Heike Tost, Brynja Magnusdottir, Stacy Steinberg, Michael Didriksen, Evald Saemundsen, Gudrun Maria Jonsdottir, Sunna Arnarsdottir, Larus S Gudmundsson, Stefan Hreidarsson
2013-02-17

No association between general cognitive ability and rare copy number variation.

Allan F McRae, Margaret J. Wright, Narelle Hansell, Nick Martin, Grant W. Montgomery
2013-02-15

Schizophrenia genetic variants are not associated with intelligence

Michael C O'Donovan, Hywel Williams, T. Scott Stroup, Engilbert Sigurdsson, Stephan Ripke
2013-07-17

A genome-wide association analysis of a broad psychosis phenotype identifies three loci for further investigation

Sarah Edkins, Cordelia Langford, Tiina Paunio, Paola Dazzan, Lieuwe de Haan, Inez Myin-Germeys, Benedicto Crespo-Facorro, Céline Bellenguez, Matti Pirinen, Sarah E. Hunt, Muriel Walshe, Elvira Bramon, Richard Bruggeman, Richard C Trembath, Panos Deloukas, Christopher G. Mathew, Cathryn Lewis, Nicholas W. Wood, Robert Plomin, Robin Murray, Peter Donnelly, Colin Freeman, Richard D Pearson, Damjan Vukcevic, Simon C Potter, Marta Di Forti, Jeremy Hall, Stephen M Lawrie, Andrew McIntosh, Roel Ophoff, Carmine Pariante, Marco M. Picchioni, Dan Rujescu, Jaana Suvisaari, Heather C Whalley, Matthew A. Brown, Aiden Corvin, Audrey Duncanson, Colin Palmer, Stephen Sawcer, Inês Barroso, Leena Peltonen-Palotie, Ina Giegling, René S. Kahn, Wiepke Cahn, Stephan Ripke, Luba Kalaydjieva, Heinrich Sauer, David Collier, Janusz A. Jankowski, Timothea Toulopoulou, Colm Mcdonald, Eugenia Kravariti, Madiha Shaikh, Sarah Tosato, Steven Bakker, Conrad Iyegbe, Assen V Jablensky, Matthias Weisbrod, Hugh S Markus, Anna Rautanen, Chris C A Spencer, Gavin Band, Amy Strange, Suzannah J. Bumpstead, Serge Dronov, Avazeh Tashakkori-Ghanbaria, Jessika E. Sussmann, Psychosis Endophenotypes International Consortium, Jenefer Blackwell
2013

The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation

Zoltán Kutalik, Jacques S Beckmann, Armand Valsesia
2013-11-12

Evidence that duplications of 22q11.2 protect against schizophrenia

Michael Gill, Michael C O'Donovan, Elliott Rees, George Kirov, James Walters, Sophie E Legge, Jennifer L. Moran, Derek W. Morris, Francis A O'Neill, Aiden Corvin, Wellcome Trust Case Control Consortium, Michele T Pato, Brien P. Riley, Patrick F Sullivan, Kenneth Kendler, Nick Craddock

Article - wd:Q97905480

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